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Hydrocodone Bitartrate and Acetaminophen - 21695-816-16 - (Hydrocodone Bitartrate and Acetaminophen)

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Drug Information of Hydrocodone Bitartrate and Acetaminophen

Product NDC: 21695-816
Proprietary Name: Hydrocodone Bitartrate and Acetaminophen
Non Proprietary Name: Hydrocodone Bitartrate and Acetaminophen
Active Ingredient(s): 167; 2.5    mg/5mL; mg/5mL & nbsp;   Hydrocodone Bitartrate and Acetaminophen
Administration Route(s): ORAL
Dosage Form(s): SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Hydrocodone Bitartrate and Acetaminophen

Product NDC: 21695-816
Labeler Name: Rebel Distributors Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040182
Marketing Category: ANDA
Start Marketing Date: 19980313

Package Information of Hydrocodone Bitartrate and Acetaminophen

Package NDC: 21695-816-16
Package Description: 473 mL in 1 BOTTLE (21695-816-16)

NDC Information of Hydrocodone Bitartrate and Acetaminophen

NDC Code 21695-816-16
Proprietary Name Hydrocodone Bitartrate and Acetaminophen
Package Description 473 mL in 1 BOTTLE (21695-816-16)
Product NDC 21695-816
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Hydrocodone Bitartrate and Acetaminophen
Dosage Form Name SOLUTION
Route Name ORAL
Start Marketing Date 19980313
Marketing Category Name ANDA
Labeler Name Rebel Distributors Corp
Substance Name ACETAMINOPHEN; HYDROCODONE BITARTRATE
Strength Number 167; 2.5
Strength Unit mg/5mL; mg/5mL
Pharmaceutical Classes Opioid Agonist [EPC],Opioid Agonists [MoA]

Complete Information of Hydrocodone Bitartrate and Acetaminophen


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